Clinical Scientist/Sr. Clinical Scientist - Oncology - Home-based anywhere in the US - FSP

Parexel; Boston (MA); Remote; USD 95,000 - 130,000; Full time

Job summary

Parexel seeks a Clinical Scientist to assist the protocol lead and study team in the clinical and scientific conduct of trials, including medical monitoring and imaging data reconciliation. The role supports one or more studies and may lead limited-scope work.

You will liaise with sites and stakeholders and ensure compliance with Parexel standards. Applicants should have oncology experience, 2+ years in medical monitoring, and a life sciences degree.

Qualifications

• Demonstrated oral and written communication skills.
• MS Office Suite experience required including Word, Excel, and PowerPoint.
• Advanced Excel skills (pivot tables, VLOOKUPs) needed.

Responsibilities

• Assist the CS Protocol Lead and study team with clinical/scientific conduct of studies (e.g., adjudication support, medical monitoring, imaging data reconciliation, preparation of meeting materials, protocol deviation management).
• Support clinical trial operational delivery for single or multiple studies; may lead a study with limited scope.
• Interact with internal and external stakeholders to support clinical study objectives and compliance with Parexel standards.

Skills

Communication skills

MS Office Suite

Advanced Excel

English proficiency

Willingness to travel

Education

Life sciences degree (Bachelors/Masters/PhD)

Alternative: Bachelor with 5+ years clinical development

Tools

None

Job description

Job Purpose:

The Clinical Scientist (CS) assists the CS Protocol Lead and study team with the clinical/scientific conduct of clinical studies (e.g., adjudication support, medical monitoring, imaging data reconciliation preparation of meeting materials, protocol deviation management).

Key Accountabilities:

May include but not limited to the following:

Clinical Trial Operational Delivery

• May support a single study or multiple studies


• May lead a study with limited scope (e.g., Survival Follow-up)


• Liaises with cross-functional lines as appropriate


• May interact with internal and external stakeholders (study sites, committees, etc.) in support of clinical study objectives

Compliance with Parexel Standards

• Complies with required training curriculum


• Completes timesheets accurately as required


• Submits expense reports as required


• Updates CV as required


• Maintains a working knowledge of and complies with Parexel processes,

ICH-GCPs and other applicable requirements

Skills:

• Demonstrated oral and written communication skills


• MS Office Suite Experience Required– including Word, Excel, and Power Point


• Advanced Excel skills required (pivot tables, v-lookups)


• Proficient in written and spoken English


• Willingness to travel as required for key company meetings

Knowledge and Experience:

• Pharmaceutical experience beneficial but not required


• Oncology experience is required


• 2 years medical monitoring experience preferred


• Experience with adjudication support, medical monitoring, imaging data reconciliation preparation of meeting materials, and protocol deviation management

Education:

• Bachelors/Masters/PhD in Life Sciences with 2+ years relevant career experience


• If no degree in Life Sciences, must have Bachelor's degree with significant experience in clinical development (>5 years)

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EEO Disclaimer

Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.